Patrick Short
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Health Information Management top 10%
Papers in
- Genetics 4
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
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- Epigenetics and DNA Methylation 1
- Co-authors
- Helen V. Firth (3 shared papers)Matthew E. Hurles (4 shared papers)Giuseppe Gallone (3 shared papers)K. Norton (1 shared paper)Lewis Vogler (1 shared paper)W Mansfield (1 shared paper)Alejandro Sifrim (2 shared papers)David Fitzpatrick (3 shared papers)
- Journals
- Nature Communications (2 papers)Nature (2 papers)Biomaterials (1 paper)Journal of Medical Genetics (1 paper)The EMBO Journal (1 paper)
- Partner nations
- United KingdomUnited StatesBelgium
In The Last Decade
Patrick Short
10 papers receiving 501 citations
Peers
Comparison fields: 5 of 98
- Genetics 150
- Health Information Management 19
- Molecular Biology 249
- Management Information Systems 33
- Cancer Research 44
Countries citing papers authored by Patrick Short
This map shows the geographic impact of Patrick Short's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Patrick Short with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Short more than expected).
Fields of papers citing papers by Patrick Short
This network shows the impact of papers produced by Patrick Short. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Patrick Short. The network helps show where Patrick Short may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Short, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 137 | |
| 2 | 2012 | 100 | |
| 3 | 1955 | 67 | |
| 4 | 1995 | 61 | |
| 5 | 2022 | 53 | |
| 6 | 2015 | 52 | |
| 7 | 2019 | 41 | |
| 8 | 2020 | 16 | |
| 9 | 2023 | 3 | |
| 10 | 2019 | 1 |
About Patrick Short
Patrick Short is a scholar working on Genetics, Molecular Biology, Cancer Research, Pediatrics, Perinatology and Child Health and Health Information Management, having authored 10 papers that have together received 531 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Epigenetics and DNA Methylation (1 paper), Science, Research, and Medicine (1 paper), Cancer Genomics and Diagnostics (1 paper), Immunotherapy and Immune Responses (1 paper), Chromosomal and Genetic Variations (1 paper) and Biomedical Ethics and Regulation (1 paper). The work is most often cited by research in Genetics (150 citations), Health Information Management (19 citations), Molecular Biology (249 citations), Management Information Systems (33 citations) and Cancer Research (44 citations). Patrick Short has collaborated with scholars based in United Kingdom, United States and Belgium. Frequent co-authors include Helen V. Firth, Matthew E. Hurles, Giuseppe Gallone, K. Norton, Lewis Vogler, W Mansfield, Alejandro Sifrim, David Fitzpatrick, Jeremy F. McRae and Caroline F. Wright. Their work appears in journals such as Nature Communications, Nature, Biomaterials, Journal of Medical Genetics and The EMBO Journal.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.